Neonatal hemolytic disease is caused by incompatibility between the baby’s and the mother’s blood types. In severe cases, it may lead to symptoms such as jaundice, anemia, restricted motor skills in hands and feet, and even heart failure, respiratory distress, and edema. It is crucial to provide scientific feeding, a balanced diet, and active treatment to prevent the worsening of the condition. Among these children with compatible blood types, 20% suffer from hemolytic diseases. Rh-negative Rh blood type is quite high, most often seen in the second child, and this hemolytic disease is relatively more dangerous.
The symptoms of neonatal jaundice and the differences between normal jaundice and abnormal jaundice that requires treatment.
Infant diarrhea may be related to factors such as indigestion, enteritis, improper feeding, and drug side effects.
Patients with kidney disease syndrome should pay attention to low-sodium, low-fat, and high-protein diets, and avoid high-sodium foods. Recommended foods include mushrooms, vegetables, and fruits.
When a newborn’s bilirubin levels are high, treatment usually includes blue light therapy and oral medication. In severe cases, intravenous anti-jaundice drugs or blood transfusions may be required. It’s important to monitor bilirubin levels and receive treatment under a doctor’s guidance to prevent serious complications such as kernicterus. Additionally, appropriate sun exposure can help lower bilirubin levels.
Galactosemia is a genetic metabolic disorder passed down through generations in humans, caused by a deficiency in the 1-phosphogalactose uridylyltransferase enzyme, which prevents infants from metabolizing lactose in milk, leading to the formation of galactose. Galactosemia is a toxic clinical diagnosis metabolic syndrome characterized by elevated blood galactose levels. Any congenital defect in any of the three related enzymes in the galactose metabolism process can lead to galactosemia.
Hydrocele is a common abdominal disease in newborns, also known as hernia, which usually requires surgical treatment.
Neonatal hemolytic disease refers to an immune hemolytic disease caused by incompatibility between the mother and baby’s blood types, leading to the destruction of the fetus’s red blood cells.
What is neonatal hemolytic disease? My child was just born a few days ago, and the doctor told us that the baby has neonatal hemolytic disease. What is this condition?
Neonatal hemolytic disease refers to the condition where the newborn’s red blood cells are destroyed by immune reactions, leading to anemia. This typically occurs when there is an incompatibility between the mother and the baby’s blood types, most commonly when the mother is O-type and the baby is A-type or B-type.
